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材料导报  2026, Vol. 40 Issue (8): 25040131-6    https://doi.org/10.11896/cldb.25040131
  金属与金属基复合材料 |
S、Mo共改性钴基复合材料的制备及析氧反应研究
谷潇, 王艺洁, 秦丽娜, 彭璇, 杜毛湛, 孙立贤*, 徐芬*
桂林电子科技大学材料科学与工程学院,广西信息材料重点实验室暨广西新能源与材料结构与性能协同创新中心,广西 桂林 541004
Study on Preparation and Oxygen Evolution Reaction Performance of S,Mo Co-modified Cobalt-based Composites
GU Xiao, WANG Yijie, QIN Lina, PENG Xuan, DU Maozhan, SUN Lixian*, XU Fen*
Guangxi Key Laboratory of Information Materials & Guangxi Collaborative Innovation Center for Structure and Properties for New Energy and Materials, School of Material Science and Engineering, Guilin University of Electronic Technology, Guilin 541004, Guangxi, China
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摘要 金属有机框架(MOFs)因其丰富的金属位点、大的比表面积和可调节的多孔结构而成为一类有前途的催化剂。然而,大多数MOFs的低电子电导率限制了它们在电催化中的应用。本工作采用两步合成法构筑Co-MOF复合催化剂。首先运用溶剂热法制备硫化的钴金属有机框架前驱体,继而利用水热反应引入Mo元素进行结构改性。优化后的Mo/S-Co-MOF催化剂表现出最佳的析氧反应(OER)催化性能,在10 mA·cm-2的电流密度下过电位为255 mV,Tafel斜率为89 mV·dec-1,且在40 h连续电解后仍保持89%的催化活性,优于文献报道的电催化剂(CoMo LDH/CNTs),相较于文献报道的CoMo LDH/CNTs催化剂,其过电位降低了11 mV,展现出更优的催化性能。而且,电荷转移电阻(Rct)较传统的Co-MOF催化剂降低了3.04 Ω,证明了S、Mo改性可调节Co的电子结构,降低电荷转移电阻,从而加快了电子传输。同时,CoMo双金属强相互作用能有效抑制电解液腐蚀,在一定程度上增强了析氧活性和耐久性。本工作可为设计低成本过渡金属基电解水催化剂提供新的思路。
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谷潇
王艺洁
秦丽娜
彭璇
杜毛湛
孙立贤
徐芬
关键词:  电催化  析氧反应(OER)  过渡金属  杂原子掺杂  金属有机框架    
Abstract: Metal-organic frameworks (MOFs) are a promising class of catalysts due to their abundant metal sites, large specific surface area and tunable porous structure. However, the low electronic conductivity of most MOFs limits their application in electrocatalysis. In thiswork, a two-step synthesis method was used to construct Co-MOF composite catalysts. The sulfided cobalt metal-organic framework precursor was first prepared using a solvothermal method, followed by the introduction of Mo elements for structural modification using a hydrothermal reaction. The optimized Mo/S-Co-MOF catalyst exhibited the best OER catalytic performance, with an overpotential of 255 mV and a Tafel slope of 89 mV·dec-1 at a current density of 10 mA·cm-2, and maintained 89% catalytic activity after 40 h of continuous electrolysis. Superior to the electrocatalysts reported in the literature (CoMo LDH/CNTs), the overpotential was reduced by 11 mV. Moreover, the charge transfer resistance (Rct) was reduced by 3.04 Ω compared with that of the conventional Co-MOF catalysts, which proved that the S, Mo modification could modulate the electronic structure of Co and reduce the charge transfer resistance, thus accelerating the electron transport. Meanwhile, the strong interaction of CoMo bimetallic can effectively inhibit the electrolyte corrosion and enhance the oxygen precipitation activity and durability to some extent. This study provides a new idea for designing low-cost transition metal-based catalysts for electrolytic water.
Key words:  electrocatalysis    oxygen evolution reaction (OER)    transition metal    heteroatom doping    metal-organic framework (MOF)
出版日期:  2026-04-25      发布日期:  2026-05-06
ZTFLH:  TQ116  
基金资助: 国家自然科学基金 (52271205;U20A20237;52371218;52101245);广西科技研发基金 (AA19182014);广西重点研发项目 (2021AB17045);桂林市科学技术研究开发项目 (20210102-4);广西八桂学者基金;漓江学者基金;广西新能源材料结构与性能协同创新中心,中德合作项目 (GZ1528)
通讯作者:  * 孙立贤,博士,桂林电子科技大学材料科学与工程学院、博/硕士研究生导师。目前主要从事制/储氢材料、相变储热材料、超级电容器电极材料、传感材料、机器学习等方面的研究。Sunlx@guet.edu.cn
徐芬,博士,桂林电子科技大学材料科学与工程学院、博/硕士研究生导师。目前主要从事制/储氢材料、相变储热材料、超级电容器电极材料、传感材料等方面的研究。xufen@guet.edu.cn   
作者简介:  谷潇,桂林电子科技大学材料科学与工程学院硕士研究生,主要从事新能源材料中的电解水析氧催化剂的制备及性能研究。
引用本文:    
谷潇, 王艺洁, 秦丽娜, 彭璇, 杜毛湛, 孙立贤, 徐芬. S、Mo共改性钴基复合材料的制备及析氧反应研究[J]. 材料导报, 2026, 40(8): 25040131-6.
GU Xiao, WANG Yijie, QIN Lina, PENG Xuan, DU Maozhan, SUN Lixian, XU Fen. Study on Preparation and Oxygen Evolution Reaction Performance of S,Mo Co-modified Cobalt-based Composites. Materials Reports, 2026, 40(8): 25040131-6.
链接本文:  
https://www.mater-rep.com/CN/10.11896/cldb.25040131  或          https://www.mater-rep.com/CN/Y2026/V40/I8/25040131
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